Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

Hum Mol Genet. 1995 Aug;4(8):1467-9. doi: 10.1093/hmg/4.8.1467.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA / genetics
  • Deafness / genetics*
  • Female
  • Genetic Markers
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation*
  • POU Domain Factors
  • Pedigree
  • Phenotype
  • Polymorphism, Single-Stranded Conformational
  • Sequence Deletion
  • Transcription Factors / genetics*
  • X Chromosome / genetics*

Substances

  • Genetic Markers
  • POU Domain Factors
  • POU3F4 protein, human
  • Transcription Factors
  • DNA